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维拉帕米在人主动脉内膜细胞培养中的抗动脉粥样硬化作用

[The antiatherosclerotic effect of verapamil in a cell culture of human aortic intima].

作者信息

Iakushkin V V, Tertov V V, Orekhov A N

出版信息

Kardiologiia. 1993;33(9):51-4, 5.

PMID:8145443
Abstract

Verapamil was examined for effects on atherosclerotic manifestations in cultured human aortic intimal cells. Addition of verapamil in a concentration of 10(-6)-10(-4) M to the cultured cells isolated from aortic atherosclerotic areas led to lower cellular lipids, suppressed cell proliferation and inhibited synthesis of collagen and cholesterol esters 24 hours after incubation. Verapamil also prevented atherogenic serum-induced accumulation of cholesterol in the cells isolated from normal aortic intimal areas. No decrease in cellular cholesterol levels was observed when the cells had been incubated with verapamil in the medium containing lipid-free serum. The findings suggest that the atherosclerotic effect of verapamil, which was seen in the experiments with animals, can be determined by the action of this drug on cellular processes.

摘要

研究了维拉帕米对培养的人主动脉内膜细胞动脉粥样硬化表现的影响。将浓度为10(-6)-10(-4)M的维拉帕米添加到从主动脉粥样硬化区域分离的培养细胞中,孵育24小时后,可降低细胞脂质、抑制细胞增殖并抑制胶原蛋白和胆固醇酯的合成。维拉帕米还可防止致动脉粥样硬化血清诱导的从正常主动脉内膜区域分离的细胞中胆固醇的积累。当细胞在不含脂质血清的培养基中与维拉帕米一起孵育时,未观察到细胞胆固醇水平降低。这些发现表明,在动物实验中观察到的维拉帕米的动脉粥样硬化作用可能由该药物对细胞过程的作用所决定。

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